Search Results - "Gamir, M. L."

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    Long-term experience of bosentan for treating ulcers and healed ulcers in systemic sclerosis patients by García de la Peña-Lefebvre, P., Rodríguez Rubio, S., Valero Expósito, M., Carmona, L., Gámir Gámir, M. L., Beltrán Gutiérrez, J., Díaz-Miguel, C., Orte Martínez, J., Zea Mendoza, A. C.

    Published in Rheumatology (Oxford, England) (01-04-2008)
    “…Objectives. Our objective was to evaluate the efficacy and tolerability of bosentan in patients with systemic sclerosis (SSc) who develop ulcers and healed…”
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    Fibrodysplasia ossificans progressiva in Spain: epidemiological, clinical, and genetic aspects by Morales-Piga, A, Bachiller-Corral, J, Trujillo-Tiebas, M.J, Villaverde-Hueso, A, Gamir-Gamir, M.L, Alonso-Ferreira, V, Vázquez-Díaz, M, Posada de la Paz, M, Ayuso-García, C

    Published in Bone (New York, N.Y.) (01-10-2012)
    “…Abstract We aimed to investigate the epidemiological determinants, clinical features, and genetic pattern of FOP in our country by evaluating the entire…”
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    Recommendations for the use of methotrexate in patients with juvenile idiopathic arthritis by Calvo, I, Antón, J, López Robledillo, J C, de Inocencio, J, Gamir, M L, Merino, R, Lacruz, L, Camacho, M, Rua, M J, Bustabad, S, Díaz Cordovés-Rego, G

    “…To develop a consensus document of recommendations for the use of methotrexate (MTX) in patients with juvenile idiopathic arthritis (JIA). A group of eleven…”
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    Reduced joint assessment vs comprehensive assessment for ultrasound detection of synovitis in juvenile idiopathic arthritis by Collado, Paz, Naredo, Esperanza, Calvo, Cristina, Gamir, Mari Luz, Calvo, Inmaculada, García, Maria Luz, Merino, Rosa, Graña, Jenaro, Bustabab, Sagrario, Garrido, Jesús

    Published in Rheumatology (Oxford, England) (01-08-2013)
    “…To propose a reduced joint power Doppler US (PDUS) assessment and provide preliminary evidence of its validity, feasibility, reliability and sensitivity to…”
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    Detection of synovitis by ultrasonography in clinically inactive juvenile idiopathic arthritis on and off medication by Collado, Paz, Gamir, María Luz, López-Robledillo, Juan Carlos, Merino, Rosa, Modesto, Consuelo, Monteagudo, Indalecio

    Published in Clinical and experimental rheumatology (01-07-2014)
    “…To determine the prevalence of abnormalities detected by ultrasonography (US) in children with juvenile idiopathic arthritis (JIA) showing clinically inactive…”
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    Efficacy and safety of canakinumab in cryopyrin-associated periodic syndromes: results from a Spanish cohort by Anton, Jordi, Calvo, Inmaculada, Fernández-Martin, Julián, Gamir, Mari Luz, Merino, Rosa, Jimenez-Treviño, Santiago, Sevilla, Belen, Cabades, Francisco, Bou, Rosa, Arostegui, Juan I

    Published in Clinical and experimental rheumatology (01-11-2015)
    “…Cryopyrin-associated periodic syndromes (CAPS) are dominantly-inherited autoinflammatory diseases. The uncontrolled IL-1β overproduction observed in these…”
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    Hypertrophic osteoarthropathy with acro-osteolysis in a patient with primary pulmonary hypertension by Sifuentes Giraldo, Walter Alberto, Ahijón Lana, María, Gallego Rivera, Ignacio, Bachiller Corral, Francisco Javier, Gámir Gámir, María Luz

    Published in Reumatologia clinica (01-07-2012)
    “…Hypertrophic osteoarthropathy is an entity characterized by a triad of periostitis of long bones, clubbing and arthritis. Radiologically there are two…”
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    DR, C4, and Bf allotypes in juvenile rheumatoid arthritis by Arnaiz-Villena, A, Gómez-Reino, J J, Gamir, M L, Regueiro, J R, Vicario, J L, Gómez-Reino, F J, Alonso, A, Fernandez-Dapica, M P, Irigoyen, M V, Mateo, I

    Published in Arthritis and rheumatism (01-11-1984)
    “…HLA-DR, C4, and Bf typing was performed in 99 patients with juvenile rheumatoid arthritis (JRA). DR1 was found with higher frequency in patients with…”
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    Selective deficiency of IgA in autoimmune diseases by Calabozo Raluy, M, Gamir Gamir, M L, Medina Luezas, J, Díaz-Miguel Pérez, C, Alonso Ruiz, A

    Published in Revista clínica espanõla (01-03-1990)
    “…A selective IgA deficiency (SD IgA) appears in a 0.15% of the population, being more frequent in autoimmune diseases. We present here eight patients presenting…”
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